Re: MS and worsening; AMALGAM under crown found!!

[Guest guest]

It sounds to me like you need some medications to control your anxiety and mood

more

than anything else.

It is normal to have things flare up a bit when you remove an amalgam under this

kind of

circumstance, it will calm down shortly. Things will be fine.

You do need to make doubly sure there is no MORE amalgam hiding in there

anywhere.

Andy

> Dear All,

>

> on Tuesday last week my dentist discovered amalgam under a very old

> gold crown.The filling was drilled out.

>

> Since Monday last week I've got a Cortisone impulse therapy (1 gramm per

> day for 10 days). This test shall act as an indicator, whether my MS

> is still inflammatory.

>

> But no improvement has occured up to now!

> Rather worsening! Due to drilled out amalgam??????

>

> What should I do concerning the amalgam??

>

> NEED HELP,IT'S THE HORROR!!

>

> Tom

>

>

>

>

>

> >

> > Dear Andy/All,

> >

> > I'm still chelating, but no (essential) improvements occured up to

> > now. Proper chelation for 26 months!!

> > See the above correspondence with Andy.

> >

> > Is it possible, that the dumping out of Hg does last so much time?

>

> It is possible.

>

> I'd suggest continuing to chelate but also looking into some other

> symptom suppression

> interventions to buy you more time or kick start the process.

> >

> > Please give hopegiving lines!

> >

> > Thanks

> > Tom

> >

> > Re; MS and worsening

> >

> >

> > Dear Andy/All,

> >

> > I'm suffering from MS since about 15 years (see message# 1513 and

> >

> > others in this group).

> >

> > Since August 2004 I'm chelating properly(!) according to Andy's

> >

> > schedule (3 days on /4 off; 6 on/8 off; I " fiddle around " for the best

> >

> > protocol...).

> >

> > After the first 2-3 months of chelating ALL MS symptoms have improved

> >

> > rapidly (I couldn't believe it!!).

> >

> > See the figure on page 52 of Amalgam Illness: Diagnosis and Treatment (

> > www.noamalgam.com ). That was the valley of what I refer to as " the

> > roller coaster

> > ride. "

> >

> > Study the figure well.

> >

> >

> > >Afterwards SOME symptoms worsened again clearly

> >

> > The roller coaster goes back up the hill after about 3 months in.

> > This is

> > exactly what you should expect to have happen.

> >

> > >(Ataxia, paresis of

> >

> > foot-lifter thus worsening of going ability)

> >

> > This condition is WORSE as before the beginning of chelation.

> >

> >

> > I'm very confused now.

> >

> > What should I do?

> >

> > Continue to chelate for at least a year.

> >

> > Try every kind of symptomatic support measure you can think of right

> > now, you

> > basically need to buy some time to try to get over the " hump " of

> > chelation

> > without too much difficulty.

> >

> > If you can get some " alterantive " medical care, you might try B1

> > injections

> > daily (200 + mg, intramuscular, they do hurt, you have to rotate sites

> > all

> > over), or vitamin C iv's. If you get the C, make SURE SURE SURE they

> > don't " help "

> > you by putting alpha lipoic acid or DMPS or DMSO or MSM or NAC (also

> > known as

> > mucomyst) in it. Vitamin C, minerals, maybe B complex, that is IT.

> >

> > Naltrexone is sometimes prescribed for MS in order to modulate T cell

> > activity. The amounts used are not large, this is something you might

> > find an open

> > minded mainstream doc willing to try if you root around for prescribing

> > information on the web.

> >

> > Also, take lots of EFA's like fish and flax oil, a lot of vitamin E

> > (1000+ IU

> > a day), and 5-10 mg of biotin 3-4 times a day, as well as 1000-2000

> > mcg of

> > molybdenum daily in addition to whatever supplement regimen you

> > already have

> > which hopefully includes water soluble antioxidants several times a day.

> >

> > Consider trying the Atkins diet. It brings relief to some and is

> > relatively

> > easy to do.

> >

> > One supplement that is quite helpful for a lot of MS sufferers is the

> > amino

> > acid l-histidine. It increases histamine so if you have allergy or

> > inflammation it can make those dramatically worse. So if you try it,

> > start with 250 mg

> > the first day, 500 the next, 750 the next, then 1000, 2000 and 3000.

> > Stop it

> > or cut the dose back if you get wheezy. it seems to help those with

> poor

> > balance the most.

> >

> > But study that figure on page 52 and keep 2 things in mind - you will

> > be on

> > the ride for a while and you need to hang on! Also note that if you

> stop

> > chelating you will get MUCH worse - chelation is what is keeping that

> > from

> > happening. Your body is trying to dump mercury right now and you need

> > to help it by

> > chelating regularly. The worsening is a natural part of how your body

> > dumps

> > the mercury, it is not due to the chelation.

> >

> > Andy . . .. . . .

> >

> >

> >

>

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